Thalassemia

Thalassemia is a blood disorder passed down through families in which the body makes an abnormal form or inadequate amount of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen. The disorder results in large numbers of red blood cells being destroyed, which leads to anemia.

  • Human Genetics of Infectious Diseases
  • Gene Action: Developmental Genetics
  • Consanguinity
  • Genetic Drift and Genetic Diseases in Populations with Reduced Numbers of Founders
  • Cloning in Research and Treatment of Human Genetic Disease
  • Genetic disorders in Embryology

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